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dc.contributor.authorWu, FIen_US
dc.contributor.authorShih, PIen_US
dc.contributor.authorShu, CFen_US
dc.contributor.authorTung, YLen_US
dc.contributor.authorChi, Yen_US
dc.date.accessioned2014-12-08T15:18:08Z-
dc.date.available2014-12-08T15:18:08Z-
dc.date.issued2005-11-01en_US
dc.identifier.issn0024-9297en_US
dc.identifier.urihttp://dx.doi.org/10.1021/ma051842ren_US
dc.identifier.urihttp://hdl.handle.net/11536/13098-
dc.description.abstractWe have synthesized a fluorene-based copolymer, PFA-OXD, which possesses bipolar charge-transporting functionalities, through the incorporation of electron-rich triphenylamine moieties and electron-deficient oxadiazole pendent groups into the polymer backbone and onto the C9 position of each fluorene repeating unit, respectively. The propeller-shaped triphenylamine units in the main chain and the rigid cardo-type OXD side chains endow this polymer with a very high glass transition temperature (306 degrees C) and good thermal stability, without sacrificing its good solution processability. Both in dilute solution and as a thin film, PFA-OXD exhibits a bright blue emission upon excitation of either the main chain or oxadiazole side chains; this phenomenon indicates that efficient energy transfer occurs from the photoexcited pendent groups to the polymer backbone. An organic light-emitting device incorporating this copolymer as the emitting layer exhibits a voltage-independent and stable blue emission having color coordinates (0.14, 0.15) at 9 V; the maximum brightness was 7128 cd m(-2) and the maximum luminance efficiency was 2.07 cd A(-1). In addition, doping PFA-OXD as a host material with 2.6 wt % of a red-emitting phosphorescent dye, Os(fppz), led to a high-brightness, highly efficient red electroluminescent device having CIE coordinates of (0.65, 0.34), a maximum brightness of 28 440 cd m(-2), and a maximum external efficiency of 9.30%.en_US
dc.language.isoen_USen_US
dc.titleHighly efficient light-emitting diodes based on fluorene copolymer consisting of triarylamine units in the main chain and oxadiazole pendent groupsen_US
dc.typeArticleen_US
dc.identifier.doi10.1021/ma051842ren_US
dc.identifier.journalMACROMOLECULESen_US
dc.citation.volume38en_US
dc.citation.issue22en_US
dc.citation.spage9028en_US
dc.citation.epage9036en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000232975900013-
dc.citation.woscount115-
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